Search research articles
Contact Us
Filters
Showing results (41-50 of 47) with videos related to
Page
of 5
Sort By:
You have reached the last page of results.
This site can display upto 47 results.
NPJ Genomic Medicine
|
March 1, 2024
Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies
Jil D Stegmann, Jeshurun C Kalanithy, Gabriel C Dworschak, et al.
European Journal of Human Genetics : EJHG
|
October 25, 2024
BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations
Angela Peron, Felice D'Arco, Kimberly A Aldinger, et al.
The Journal of Clinical Investigation
|
March 28, 2023
CERT1 mutations perturb human development by disrupting sphingolipid homeostasis
Charlotte Gehin, Museer A Lone, Winston Lee, et al.
American Journal of Human Genetics
|
October 9, 2021
Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss
Elodie M Richard, Somayeh Bakhtiari, Ashley P L Marsh, et al.
American Journal of Human Genetics
|
April 8, 2022
Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome
Sarah E M Stephenson, Gregory Costain, Laura E R Blok, et al.
The Journal of Clinical Investigation
|
November 14, 2023
Spliceosome malfunction causes neurodevelopmental disorders with overlapping features
Dong Li, Qin Wang, Allan Bayat, et al.
Autophagy
|
February 26, 2021
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)<sup>1</sup>
Daniel J Klionsky, Amal Kamal Abdel-Aziz, Sara Abdelfatah, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 47) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 47 results.
NPJ Genomic Medicine
|
March 1, 2024
Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies
Jil D Stegmann, Jeshurun C Kalanithy, Gabriel C Dworschak, et al.
European Journal of Human Genetics : EJHG
|
October 25, 2024
BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations
Angela Peron, Felice D'Arco, Kimberly A Aldinger, et al.
The Journal of Clinical Investigation
|
March 28, 2023
CERT1 mutations perturb human development by disrupting sphingolipid homeostasis
Charlotte Gehin, Museer A Lone, Winston Lee, et al.
American Journal of Human Genetics
|
October 9, 2021
Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss
Elodie M Richard, Somayeh Bakhtiari, Ashley P L Marsh, et al.
American Journal of Human Genetics
|
April 8, 2022
Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome
Sarah E M Stephenson, Gregory Costain, Laura E R Blok, et al.
The Journal of Clinical Investigation
|
November 14, 2023
Spliceosome malfunction causes neurodevelopmental disorders with overlapping features
Dong Li, Qin Wang, Allan Bayat, et al.
Autophagy
|
February 26, 2021
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)<sup>1</sup>
Daniel J Klionsky, Amal Kamal Abdel-Aziz, Sara Abdelfatah, et al.
Page
of 5